A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5899788



Internal ID22674922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:186464274..186465413hg38UCSC Ensembl
chr3:186182063..186183202hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg381140
hg191140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17412592
Samples
Known GenesLOC253573
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5899788
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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